我国水事纠纷解决机制探析

水事纠纷解决机制是一系列水事纠纷解决方式所组成的整体,该机制是民事主体或行政区域水资源权利受到侵害,以及遭受水污染侵权损害的重要救济途径。虽然我国相关法律对水事纠纷的解决方式已作出规定,但是这些法律规定较为分散、不系统,还没有形成一个有机的整体,造成运用该机制解决水事纠纷的效果较差。为了保障水事纠纷及时、有效地得以解决,完善我国的水事纠纷解决机制已迫在眉睫。     

Assessing water quality of drinking water distribution system in the South Taiwan

This investigation conducted a full-scale survey the drinking water distribution system in Kaohsiung city, Taiwan. The aim was to investigate whether the distribution system was capable of maintaining high water quality from the water treatment facilities through to the end user. The results showed that the distribution system can maintain high water quality, except for suitable chlorine residuals. The authors plotted chlorine residual contour maps to identify areas with low chlorine residuals, helping them prioritize sections that must be flushed or renewal. The contour maps also provide sufficient and clear information for locating booster chlorination stations. Contour maps enable water facilities to identify how water quality decays in the distribution systems and the locations of such decay. Water quality decay can be caused by properties of pipeline materials, hydraulic conditions, and/or biofilm thickness. However, understanding the exact reasons is unnecessary because the contour maps provide sufficient information for trouble-shooting the distribution systems.     

上海与伦敦城市绿地的生态功能及管理对策比较研究

在资料收集及实地采样调查的基础上 ,文章对上海与伦敦城市绿地的生态功能及管理对策进行了比较分析 ,指出了上海城市绿地建设及管理中的一些优点及不足之处。     

地震台站体应变观测资料处理系统简介

介绍了新近研制的地震台站体应变观测资料的日常处理系统 ;简要地介绍了该系统及其数据库的结构以及各功能模块的作用。     

底泥中重金属毒性的室内孔隙水分析技术

根据孔隙水中重金属的浓度可以判定底泥中重金属的毒性但获得真正的底泥孔隙水十分困难。本文提供了一套简便易行的室内原状孔隙水取样技术,将碳化硅砂芯埋入底泥,添加表层水并静置９０ｄ,通过渗滤获得孔隙水,测定孔隙水中重的浓度,所得结果与微生态系统暴露试验中生物指示的重金属的毒性大小相吻合,与生物积累重金属的浓度显著正相关。     

对重庆城镇网络建设的探讨

在分析重庆直辖市城镇化现状的基础上,针对重庆城镇网络中存在的问题,依据重庆发展城镇网络的优势,提出了建立新的城镇网络扔基本思路和构想,相关的对策与建议。     

亚铵法制浆黑液作肥料对水环境影响的研究

通过亚铵法制浆蒸煮黑液直接作农肥施于水稻田的研究,给出了不同施肥方式连续数天田间水和渗滤水中黑液污染物变化情况,定量描述了黑液作肥料直接施于水稻田对水环境的影响。     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

遗传和模拟退火算法在水质模型参数确定中的应用简介

水质模型参数的确定是构建水质模型的基础。相对于传统优化方法,现代优化算法的优势日趋明显。本文在基于现代优化算法的水质模型参数确定研究背景下,介绍了具有代表性的遗传算法和模拟退火算法,并对该两种算法的应用现状进行综述,旨在推进该领域的进一步探索。     

红外分光光度法测定水和废水中油类的改进

本文对红外分光光度法测定水和废水中的油类的萃取和吸附操作进行了改进。结果表明,该方法的精密度和准确度能达到国家标准的要求,且操作更加方便、快捷,可以应用于日常环境监测分析。